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Association between Glutathione S-Transferase T1, M1, and P1 Genotypes and the Risk of Colorectal Cancer
Glutathione S-transferases (GSTs) are enzymes which play an important role in the neutralization of toxic compounds and eradication of electrophilic carcinogens. Genetic polymorphisms within the genes encoding for GSTs may therefore cause variations in their enzyme activity, which may in turn influe...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Academy of Medical Sciences
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4234915/ https://www.ncbi.nlm.nih.gov/pubmed/25408579 http://dx.doi.org/10.3346/jkms.2014.29.11.1488 |
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author | Cong, Ning Liu, Lisheng Xie, Ying Shao, Wenbo Song, Jinlong |
author_facet | Cong, Ning Liu, Lisheng Xie, Ying Shao, Wenbo Song, Jinlong |
author_sort | Cong, Ning |
collection | PubMed |
description | Glutathione S-transferases (GSTs) are enzymes which play an important role in the neutralization of toxic compounds and eradication of electrophilic carcinogens. Genetic polymorphisms within the genes encoding for GSTs may therefore cause variations in their enzyme activity, which may in turn influence the interindividual susceptibility to cancers. In this study, we aimed to investigate the association between genetic polymorphisms of GSTT1, GSTM1, and GSTP1 and the risk of colorectal cancer (CRC) in 264 cases and 317 controls in a Chinese population. Genotyping was performed by using multiplex PCR (for GSTT1 and GSTM1) and PCR-RFLP (for GSTP1) methods. The association between the polymorphic genotypes and CRC risk was evaluated by deriving odds ratios (ORs) and 95% confidence intervals (CIs) using unconditional logistic regression analysis. Our results showed that individuals with GSTT1 and GSTM1 null genotypes exhibited a higher risk of CRC (GSTT1, OR,1.66; 95% CI, 1.20-2.31, P=0.003; GSTM1, OR,1.57; 95% CI,1.13-2.18, P=0.007), while no association was observed for GSTP1 (P(heterozygous)=0.790 or P(variant)=0.261). Furthermore, individuals who simultaneously carried the null genotypes for both GSTT1 and GSTM1 showed a stronger risk association (OR, 1.95; 95% CI, 1.33-2.85; P<0.001). In conclusion, the GSTT1 and GSTM1 polymorphisms, but not GSTP1, may modulate the CRC risk among Chinese. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-4234915 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Korean Academy of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-42349152014-11-18 Association between Glutathione S-Transferase T1, M1, and P1 Genotypes and the Risk of Colorectal Cancer Cong, Ning Liu, Lisheng Xie, Ying Shao, Wenbo Song, Jinlong J Korean Med Sci Original Article Glutathione S-transferases (GSTs) are enzymes which play an important role in the neutralization of toxic compounds and eradication of electrophilic carcinogens. Genetic polymorphisms within the genes encoding for GSTs may therefore cause variations in their enzyme activity, which may in turn influence the interindividual susceptibility to cancers. In this study, we aimed to investigate the association between genetic polymorphisms of GSTT1, GSTM1, and GSTP1 and the risk of colorectal cancer (CRC) in 264 cases and 317 controls in a Chinese population. Genotyping was performed by using multiplex PCR (for GSTT1 and GSTM1) and PCR-RFLP (for GSTP1) methods. The association between the polymorphic genotypes and CRC risk was evaluated by deriving odds ratios (ORs) and 95% confidence intervals (CIs) using unconditional logistic regression analysis. Our results showed that individuals with GSTT1 and GSTM1 null genotypes exhibited a higher risk of CRC (GSTT1, OR,1.66; 95% CI, 1.20-2.31, P=0.003; GSTM1, OR,1.57; 95% CI,1.13-2.18, P=0.007), while no association was observed for GSTP1 (P(heterozygous)=0.790 or P(variant)=0.261). Furthermore, individuals who simultaneously carried the null genotypes for both GSTT1 and GSTM1 showed a stronger risk association (OR, 1.95; 95% CI, 1.33-2.85; P<0.001). In conclusion, the GSTT1 and GSTM1 polymorphisms, but not GSTP1, may modulate the CRC risk among Chinese. GRAPHICAL ABSTRACT: [Image: see text] The Korean Academy of Medical Sciences 2014-11 2014-11-04 /pmc/articles/PMC4234915/ /pubmed/25408579 http://dx.doi.org/10.3346/jkms.2014.29.11.1488 Text en © 2014 The Korean Academy of Medical Sciences. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Cong, Ning Liu, Lisheng Xie, Ying Shao, Wenbo Song, Jinlong Association between Glutathione S-Transferase T1, M1, and P1 Genotypes and the Risk of Colorectal Cancer |
title | Association between Glutathione S-Transferase T1, M1, and P1 Genotypes and the Risk of Colorectal Cancer |
title_full | Association between Glutathione S-Transferase T1, M1, and P1 Genotypes and the Risk of Colorectal Cancer |
title_fullStr | Association between Glutathione S-Transferase T1, M1, and P1 Genotypes and the Risk of Colorectal Cancer |
title_full_unstemmed | Association between Glutathione S-Transferase T1, M1, and P1 Genotypes and the Risk of Colorectal Cancer |
title_short | Association between Glutathione S-Transferase T1, M1, and P1 Genotypes and the Risk of Colorectal Cancer |
title_sort | association between glutathione s-transferase t1, m1, and p1 genotypes and the risk of colorectal cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4234915/ https://www.ncbi.nlm.nih.gov/pubmed/25408579 http://dx.doi.org/10.3346/jkms.2014.29.11.1488 |
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